Acacia Basic Science IBC Services
Acacia Safety Consulting provides biological, chemical, and OSHA safety support for biopharma and academic institutions, CROs, hospitals, and clinics.
We are committed to providing our clients with customized, sustainable, and effective EHS solutions that are adaptable to various work environments, ensuring the well-being of employees and the environment.
Complying with NIH Guidelines is mandatory for all recombinant research conducted at NIH-funded sites, and the first step towards compliance is establishing an Institutional Biosafety Committee (IBC).
Our biosafety consultants have extensive experience in all aspects of setting up, managing, and reviewing research protocols for basic science research and gene and cell therapy clinical trials, including:
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Registering an IBC with the NIH
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Policies and Procedures
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IBC Applications / Biological Use Authorization Forms
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Document Preparation
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Facility Suitability Assessments
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NIH Guidelines Applicability and Requirements
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Biosafety Training: Storage, Handling, Administration, and Disposal
We can help you manage your IBC in a way that best fits your organization by providing any or all of the necessary roles for effective IBC functioning:
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IBC Chair
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Biological Safety Officer
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IBC Coordinator
An IBC is most effective when integrated into a specific facility's established operations. We take the time to understand your programs and organizational structure, customizing the IBC to seamlessly fit within your organization.
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We offer varying levels of support based on your needs. Whether you require assistance with the initial IBC setup, training for employee self-sufficiency, or continuous ongoing management of the program, we're here to help.
Established IBC Support for Clinical Trial Sites
We not only assist with IBC administration but also support CROs and study sponsors conducting gene and cell therapy clinical trials at sites with an established IBC. Specifically, we help site clinical trial coordinators submit their local IBC applications in time for upcoming meetings. Advantages of this approach include:
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Faster Site IBC Approvals: Acacia Safety Consulting manages the technical aspects of IBC application filings, freeing up time for busy Clinical Trial Coordinators. Our expertise in gene and cell therapy, combined with our experience in the IBC approval process, helps expedite your clinical trial site's approvals and minimize delays.
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Ongoing Site Support: We provide on-call site support from trial initiation to completion. Our objective is to promptly address and resolve any concerns or challenges that may arise.